| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42075816-42076191 | Rare:102 | ||||
| chr19:42132402-42132637 | Rare:47 | ||||
| chr19:42302310-42302405 | Rare:34 | ||||
| chr19:42302416-42302634 | Rare:63 | ||||
| chr19:43527182-43527308 | Common:4; Rare:49; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr19:43575462-43575818 | Common:2; Rare:94 | ||||
| chr19:43596132-43596450 | Common:2; Rare:100 | ||||
| chr19:43670121-43670365 | Common:2; Rare:63 | ||||
| chr19:43754850-43755108 | Common:3; Rare:102 | ||||
| chr19:43780957-43781164 | Rare:43 | ||||
| chr19:43827204-43827433 | Common:2; Rare:48 | ||||
| chr19:43901755-43901925 | Common:3; Rare:36 | ||||
| chr19:43935231-43935356 | Common:2; Rare:35 | ||||
| chr19:43951035-43951247 | Common:2; Rare:53 | ||||
| chr19:44002783-44002986 | Common:4; Rare:52 |